A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524411



Internal ID15105018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:101190975..101377649hg38UCSC Ensembl
InnerchrX:100445964..100632637hg19UCSC Ensembl
InnerchrX:100332620..100519293hg18UCSC Ensembl
InnerchrX:100252109..100438782hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38186675
hg19186674
hg18186674
hg17186674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700333
Samples
Known GenesBTK, DRP2, TAF7L, TIMM8A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524411
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer